About this opportunity
Regeneron Pharmaceuticals, Inc (USA) lists this Senior Manager, Clinical Scientist, Cardiovascular/Specialty Medicine opportunity in village of tarrytown, New York. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Build our future together: At Regeneron, we use science and innovation to develop life‑changing medicines for people with serious diseases. We are seeking a Senior Manager, Clinical Sciences (Internal Medicine) to join our Clinical Sciences team, supporting our global clinical development programs in cardiovascular, renal, and metabolic disease. In this role, you will help design, execute, and interpret clinical studies, safeguarding data integrity and patient safety while collaborating with Medical Directors and cross‑functional study teams. This position offers the opportunity to contribute to a fast‑growing, science‑driven organization making a meaningful difference to patients worldwide.
When & where: Location: Tarrytown, NY, Warren, NJ, Cambridge, MA Work model/flexibility: Primarily on‑site with hybrid flexibility
Discover your role
Partner with Medical Directors to deliver the scientific expertise needed to design and run clinical studies
Contribute to clinical study teams, program team meetings, advisory boards, steering committees, and data/safety monitoring meetings
Support early and/or late‑phase studies by helping develop protocol synopses and authoring or reviewing protocols and amendments
Author and review study documents, including medical monitoring plans, SAPs, informed consents, and clinical study report sections
Perform clinical and medical data review, including safety monitoring, to protect patient safety
Work with internal functions and external vendors to promote study integrity and consistent data review practices
Identify critical risks and recommend mitigations by analyzing how study objectives and design affect data analysis
Build and maintain deep knowledge of the disease area, mechanism of action, and drug landscape, while upholding FDA, EMA, ICH, and GCP standards
This role requires
MS/PhD/PharmD in a related field with 8+ years of pharmaceutical clinical drug development experience (other levels considered depending on experience)
Preferred: Experience in one or more of the following therapeutic areas: cardiovascular, renal, or metabolic disease
Preferred: Track record of clinical trial process improvements
Proven knowledge of the drug development process, GCP, ICH guidelines, study design, and clinical research methodology
Strong medical writing, analytical, and presentation skills, with the ability to communicate clear, concise messages
Demonstrated ability to influence within a team and cross‑functionally in a matrix environment
Strong problem‑solving and interpersonal skills, with the ability to resolve complex issues creatively and independently
Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role
annual bonuses or other incentive plans
equity awards
pension or retirement benefits
401(k) company match
health and wellness programs
fitness centers
insurance benefits (e.g. medical, dental, vision, life and disability)
paid time off
family support benefits
For additional information about Regeneron benefits in the U.S., please visit For other locations, additional information will be provided during the recruitment process.
Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site.
As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.
For jobs in Canada: this posting is for an existing position.
Salary Range (annually) $150,500.00 - $245,500.00
Regeneron is a leading biotechnology company that invents life-transforming medicines for people with serious diseases. Founded and led for over 30 years by physician‑scientists, our unique ability to repeatedly and consistently translate science into medicine has led to nine FDA‑approved treatments and numerous product candidates in development, almost all of which were homegrown in our laboratories. Our medicines and pipeline are designed to help patients with eye diseases, allergic and inflammatory diseases, cancer, cardiovascular and metabolic diseases, neurology, infectious diseases and rare diseases.
Regeneron is also proud of award winning culture of innovation, being recognized as a Great Place to Work in 2021, Fast Company’s Best Workplace for Innovators in 2020, and Forbes JUST companies in 2020, among others.
We are committed to building a workplace with an inclusive culture.
Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.
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Who can apply
Review the original listing for work authorization, qualifications and employer requirements.